A citation-based method for searching scientific literature

Xiang Zhan, Ni Zhao, Anna Plantinga, Timothy A Thornton, Karen N Conneely, Michael P Epstein, Michael C Wu. Genetics 2017
Times Cited: 21







List of co-cited articles
130 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011
61

Rare-variant association analysis: study designs and statistical tests.
Seunggeung Lee, Gonçalo R Abecasis, Michael Boehnke, Xihong Lin. Am J Hum Genet 2014
527
42

Pleiotropy in complex traits: challenges and strategies.
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
558
38

A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.
K Alaine Broadaway, David J Cutler, Richard Duncan, Jacob L Moore, Erin B Ware, Min A Jhun, Lawrence F Bielak, Wei Zhao, Jennifer A Smith, Patricia A Peyser,[...]. Am J Hum Genet 2016
37
38

Sequence Kernel Association Test of Multiple Continuous Phenotypes.
Baolin Wu, James S Pankow. Genet Epidemiol 2016
26
33

A groupwise association test for rare mutations using a weighted sum statistic.
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
769
33

Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.
Diptavo Dutta, Laura Scott, Michael Boehnke, Seunggeun Lee. Genet Epidemiol 2019
22
33


Multivariate phenotype association analysis by marker-set kernel machine regression.
Arnab Maity, Patrick F Sullivan, Jun-Ying Tzeng. Genet Epidemiol 2012
60
28

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
Seunggeun Lee, Mary J Emond, Michael J Bamshad, Kathleen C Barnes, Mark J Rieder, Deborah A Nickerson, David C Christiani, Mark M Wurfel, Xihong Lin. Am J Hum Genet 2012
549
28

Multi-trait analysis of genome-wide association summary statistics using MTAG.
Patrick Turley, Raymond K Walters, Omeed Maghzian, Aysu Okbay, James J Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A Furlotte,[...]. Nat Genet 2018
261
28

Kernel machine SNP-set testing under multiple candidate kernels.
Michael C Wu, Arnab Maity, Seunggeun Lee, Elizabeth M Simmons, Quaker E Harmon, Xinyi Lin, Stephanie M Engel, Jeffrey J Molldrem, Paul M Armistead. Genet Epidemiol 2013
42
23

Rare variant association test with multiple phenotypes.
Selyeong Lee, Sungho Won, Young Jin Kim, Yongkang Kim, Bong-Jo Kim, Taesung Park. Genet Epidemiol 2017
13
38

A mixed-model approach for genome-wide association studies of correlated traits in structured populations.
Arthur Korte, Bjarni J Vilhjálmsson, Vincent Segura, Alexander Platt, Quan Long, Magnus Nordborg. Nat Genet 2012
221
23


Optimal tests for rare variant effects in sequencing association studies.
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
402
19


Maximizing the power of principal-component analysis of correlated phenotypes in genome-wide association studies.
Hugues Aschard, Bjarni J Vilhjálmsson, Nicolas Greliche, Pierre-Emmanuel Morange, David-Alexandre Trégouët, Peter Kraft. Am J Hum Genet 2014
94
19

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects.
Jianping Sun, Karim Oualkacha, Vincenzo Forgetta, Hou-Feng Zheng, J Brent Richards, Antonio Ciampi, Celia Mt Greenwood. Eur J Hum Genet 2016
16
25

Calibrating a coalescent simulation of human genome sequence variation.
Stephen F Schaffner, Catherine Foo, Stacey Gabriel, David Reich, Mark J Daly, David Altshuler. Genome Res 2005
471
19

Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.
Iuliana Ionita-Laza, Marinela Capanu, Silvia De Rubeis, Kenneth McCallum, Joseph D Buxbaum. PLoS Genet 2014
32
19

A multivariate test of association.
Manuel A R Ferreira, Shaun M Purcell. Bioinformatics 2009
156
19



Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension.
Xiaofeng Zhu, Tao Feng, Bamidele O Tayo, Jingjing Liang, J Hunter Young, Nora Franceschini, Jennifer A Smith, Lisa R Yanek, Yan V Sun, Todd L Edwards,[...]. Am J Hum Genet 2015
166
19

MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS.
Paul F O'Reilly, Clive J Hoggart, Yotsawat Pomyen, Federico C F Calboli, Paul Elliott, Marjo-Riitta Jarvelin, Lachlan J M Coin. PLoS One 2012
215
19

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
14

USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.
Debashree Ray, James S Pankow, Saonli Basu. Genet Epidemiol 2016
26
14

Abundant pleiotropy in human complex diseases and traits.
Shanya Sivakumaran, Felix Agakov, Evropi Theodoratou, James G Prendergast, Lina Zgaga, Teri Manolio, Igor Rudan, Paul McKeigue, James F Wilson, Harry Campbell. Am J Hum Genet 2011
319
14

PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.
Janina S Ried, Angela Döring, Konrad Oexle, Christa Meisinger, Juliane Winkelmann, Norman Klopp, Thomas Meitinger, Annette Peters, Karsten Suhre, H-Erich Wichmann,[...]. Genet Epidemiol 2012
16
18

Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT).
Eugene Urrutia, Seunggeun Lee, Arnab Maity, Ni Zhao, Judong Shen, Yun Li, Michael C Wu. Stat Interface 2015
8
37


Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method.
Qi Yan, Daniel E Weeks, Juan C Celedón, Hemant K Tiwari, Bingshan Li, Xiaojing Wang, Wan-Yu Lin, Xiang-Yang Lou, Guimin Gao, Wei Chen,[...]. Genetics 2015
11
27

Sequence kernel association test for quantitative traits in family samples.
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
156
14





Sequence kernel association tests for the combined effect of rare and common variants.
Iuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, Joseph D Buxbaum, Xihong Lin. Am J Hum Genet 2013
276
14

Powerful SNP-set analysis for case-control genome-wide association studies.
Michael C Wu, Peter Kraft, Michael P Epstein, Deanne M Taylor, Stephen J Chanock, David J Hunter, Xihong Lin. Am J Hum Genet 2010
387
14

Prioritizing individual genetic variants after kernel machine testing using variable selection.
Qianchuan He, Tianxi Cai, Yang Liu, Ni Zhao, Quaker E Harmon, Lynn M Almli, Elisabeth B Binder, Stephanie M Engel, Kerry J Ressler, Karen N Conneely,[...]. Genet Epidemiol 2016
9
33

Statistical analysis strategies for association studies involving rare variants.
Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J Schork. Nat Rev Genet 2010
323
14

Natural variations and genome-wide association studies in crop plants.
Xuehui Huang, Bin Han. Annu Rev Plant Biol 2014
283
14

Analyzing Association Mapping in Pedigree-Based GWAS Using a Penalized Multitrait Mixed Model.
Jin Liu, Can Yang, Xingjie Shi, Cong Li, Jian Huang, Hongyu Zhao, Shuangge Ma. Genet Epidemiol 2016
8
37

Multiple-trait genome-wide association study based on principal component analysis for residual covariance matrix.
H Gao, Y Wu, T Zhang, Y Wu, L Jiang, J Zhan, J Li, R Yang. Heredity (Edinb) 2014
10
30


An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.
Vincent Segura, Bjarni J Vilhjálmsson, Alexander Platt, Arthur Korte, Ümit Seren, Quan Long, Magnus Nordborg. Nat Genet 2012
413
14


Methods for meta-analysis of multiple traits using GWAS summary statistics.
Debashree Ray, Michael Boehnke. Genet Epidemiol 2018
26
14

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.